Canonical Allele Identifier: PA2828800330
Gene: NPR2 HGNC NCBI
ClinVar RCV:
RCV003781101
ClinVar Variation:
2925447
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365852.1:p.Thr297Met
CA373369142
NM_001378923.1:c.890C>T